Jewish Genetic Conditions Are in Our DNA. They're Also in Our Power to Change.

SLC1A4 Deficiency is a devastating neurological disorder affecting Jewish families around the world. Roughly 1 out of 100 Ashkenazi Jews are carriers and most don't know it. Together, we can we can eradicate this genetic condition.

SLC1A4 family
Profound Neurological Impact
Life-limiting diagnosis
Undetected by Screening
Excluded from many genetic testing panels
No Available Treatments
No therapies currently exist

Advancing the Science, Accelerating the Cure

Every dollar directly funds research that will lead to treatments for SLC1A4 Deficiency and advocacy to eradicate it through genetic testing

How Your Donation Is Used

100%
Goes directly to research
Laboratory & Animal Models
Building the tools needed to study and test therapies
Therapeutic Candidate Testing
Identifying and evaluating potential treatments
Clinical Trials
Moving the most promising treatments into human trials
Advocacy
Promoting inclusion on genetic testing panels
Administrative costs are covered separately — so every dollar you give goes to science and advocacy.

Roadmap to a Cure

Gene Identified Complete
First Patients Diagnosed Complete
3
Natural History Study In Progress
4
Develop Laboratory Model Next
5
Investigate Therapies
6
Begin Clinical Trials